Literature DB >> 15242938

Longitudinal profile of immunoglobulin G (IgG), IgM, and IgA antibodies against the severe acute respiratory syndrome (SARS) coronavirus nucleocapsid protein in patients with pneumonia due to the SARS coronavirus.

Patrick C Y Woo1, Susanna K P Lau, Beatrice H L Wong, Kwok-hung Chan, Chung-ming Chu, Hoi-wah Tsoi, Yi Huang, J S Malik Peiris, Kwok-yung Yuen.   

Abstract

By using a recombinant severe acute respiratory syndrome coronavirus (SARS-CoV) nucleocapsid protein-based enzyme-linked immunosorbent assay (ELISA) and serum specimens serially collected (from day 0 to day 240 after symptom onset) from patients with pneumonia due to SARS-CoV, we analyzed the longitudinal profiles of immunoglobulin G (IgG), IgM, and IgA antibodies against the SARS-CoV nucleocapsid protein in patients with pneumonia due to SARS-CoV. For IgG, the median optical density at 450 nm (OD450) turned positive at day 17 and a biphasic response was observed. At day 240, all patients were still positive for anti-nucleocapsid protein IgG antibody. For IgM, the median OD450 turned positive at day 20.5, peaked at about day 80, and fell to below the baseline level at about day 180. At day 240, 36% of the patients were still positive for anti-nucleocapsid protein IgM antibody. For IgA, the median OD450 turned positive at day 17, peaked at about day 50, and fell to below the baseline level at about day 180. At day 240, 36% of the patients were still positive for anti-nucleocapsid protein IgA antibody. The time of seroconversion detected by the recombinant SARS-CoV nucleocapsid protein-based ELISA and that detected by indirect immunofluorescence assay were similar. The median times of seroconversion for IgG, IgM, and IgA detected by the indirect immunofluorescence assay were 17 days (17 days by ELISA), 16.5 days (20.5 days by ELISA), and 17.5 days (17 days by ELISA), respectively, after disease onset. One, four, and one of the six patients who died did not produce any IgG, IgM, and IgA antibodies against the nucleocapsid protein of SARS-CoV, respectively, although these antibodies were detected in all six patients by the indirect immunofluorescence assay. Further studies should be performed to see whether SARS-CoV nucleocapsid protein antibody positivity has any prognostic significance.

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Year:  2004        PMID: 15242938      PMCID: PMC440610          DOI: 10.1128/CDLI.11.4.665-668.2004

Source DB:  PubMed          Journal:  Clin Diagn Lab Immunol        ISSN: 1071-412X


  12 in total

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5.  Detection of specific antibodies to severe acute respiratory syndrome (SARS) coronavirus nucleocapsid protein for serodiagnosis of SARS coronavirus pneumonia.

Authors:  Patrick C Y Woo; Susanna K P Lau; Beatrice H L Wong; Hoi-wah Tsoi; Ami M Y Fung; Kwok-hung Chan; Victoria K P Tam; J S Malik Peiris; Kwok-yung Yuen
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10.  Relative rates of non-pneumonic SARS coronavirus infection and SARS coronavirus pneumonia.

Authors:  Patrick C Y Woo; Susanna K P Lau; Hoi-wah Tsoi; Kwok-hung Chan; Beatrice H L Wong; Xiao-yan Che; Victoria K P Tam; Sidney C F Tam; Vincent C C Cheng; Ivan F N Hung; Samson S Y Wong; Bo-jian Zheng; Yi Guan; Kwok-yung Yuen
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  79 in total

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Journal:  J Clin Microbiol       Date:  2005-07       Impact factor: 5.948

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5.  Detection of severe acute respiratory syndrome (SARS) coronavirus nucleocapsid protein in sars patients by enzyme-linked immunosorbent assay.

Authors:  Susanna K P Lau; Patrick C Y Woo; Beatrice H L Wong; Hoi-Wah Tsoi; Gibson K S Woo; Rosana W S Poon; Kwok-Hung Chan; William I Wei; J S Malik Peiris; Kwok-Yung Yuen
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